Walzel H, Ringel B, Jenssen H L, Mix E, Franz H, Ziska P
Arch Geschwulstforsch. 1984;54(6):451-61.
Crude 3M KCl extracts prepared from tumor tissue and ascitic tumor cells of methylnitrosourea-induced fibrosarcoma of CBA mice or of a human stomach adenocarcinoma were gelfiltrated on Ultrogel AcA 34. Single fractions of these preparations were incubated with spleen cells of tumor bearing mice or blood peripheral lymphocytes. The response was detected by MEM-technique. Antigenic activities were found in molecular weight ranges from 200 to 300 kD (P1) and from 40 to 70 kD (P2). Single glycoproteins of the P1- and P2-fractions could be separated by affinity chromatography on immobilized D-galactose specific mistletoe lectin I, as detected by electrophoresis on microgradient gels (1.2-40%) or on SDS polyacrylamide slab gels. Especially the isolated glycoproteins of the P1-fractions are responsible for the observed antigenic reactivity, assayed in vitro by the MEM-technique and in vivo by foot pad swelling test.
从甲基亚硝基脲诱导的CBA小鼠纤维肉瘤或人胃腺癌的肿瘤组织及腹水肿瘤细胞制备的粗制3M KCl提取物,在Ultrogel AcA 34上进行凝胶过滤。将这些制剂的单个组分与荷瘤小鼠的脾细胞或外周血淋巴细胞一起孵育。通过MEM技术检测反应。在分子量范围为200至300 kD(P1)和40至70 kD(P2)中发现了抗原活性。通过在固定化D-半乳糖特异性槲寄生凝集素I上进行亲和层析,可以分离P1和P2组分的单个糖蛋白,这通过在微梯度凝胶(1.2 - 40%)或SDS聚丙烯酰胺平板凝胶上的电泳检测。特别是P1组分中分离出的糖蛋白负责观察到的抗原反应性,通过MEM技术在体外测定,并通过足垫肿胀试验在体内测定。